A method for isolating and cultivating porcine pseudorabies virus
A porcine pseudorabies virus inoculation technology, applied in the field of isolation and cultivation of porcine pseudorabies virus, can solve the problems of low virus titer, cell death shedding, difficult isolation and cultivation of porcine pseudorabies virus, etc.
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Embodiment 1
[0028] Example 1 Isolation and cultivation of porcine pseudorabies virus SD2011-03 strain
[0029] 1) Disease material collection: select the tonsil, spleen, lymph node or brainstem tissue of pigs with porcine pseudorabies virus positive proved by PCR method. 2) Disease material treatment: Grind about 1 g of disease material with 5 mL of sterile DMEM solution containing antibiotics at a grinding temperature of 0-4°C; then freeze and thaw the grinding liquid at -70°C for 3 times, and centrifuge at 10,000 rpm for 5 Minutes, take the supernatant, discard the precipitate, take the supernatant to extract the total RNA, and perform RT-PCR amplification. A positive sample can be amplified to obtain a specific band with a size of 346bp, such as figure 1 shown. The supernatant of the disease material tested as positive was filtered and sterilized with a 0.22 μm sterile filter, and the supernatant was prepared and stored below -70°C for later use.
[0030] 3) Inoculate 1 mL of the sup...
Embodiment 2
[0039] The PCR identification of embodiment 2 porcine pseudorabies virus
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